72016-05-8 Usage
Uses
Used in Pharmaceutical Production:
1H,1H,2H,3H-Nonafluorohept-2-en-1-ol is used as an intermediate in the synthesis of various pharmaceuticals for its unique chemical properties and reactivity. Its high thermal stability and chemical resistance make it a valuable component in the development of new drugs.
Used in Chemical Reactions:
1H,1H,2H,3H-Nonafluorohept-2-en-1-ol is used as a reactant in specialized chemical reactions due to its alkene and alcohol functionalities. Its reactivity allows for the creation of new compounds with potential applications in various industries.
Used in Industrial Applications:
1H,1H,2H,3H-Nonafluorohept-2-en-1-ol is used in the production of certain industrial materials, leveraging its high thermal stability and chemical resistance. This makes it suitable for applications where materials need to withstand extreme conditions.
Used in Research and Development:
1H,1H,2H,3H-Nonafluorohept-2-en-1-ol is used as a research compound in scientific studies, particularly in the field of fluorochemistry. Its unique properties and potential biological activity make it an interesting subject for further exploration and potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 72016-05-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,0,1 and 6 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 72016-05:
(7*7)+(6*2)+(5*0)+(4*1)+(3*6)+(2*0)+(1*5)=88
88 % 10 = 8
So 72016-05-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H5F9O/c8-4(9,2-1-3-17)5(10,11)6(12,13)7(14,15)16/h1-2,17H,3H2/b2-1+
72016-05-8Relevant academic research and scientific papers
Ultrasound-Promoted Selective Perfluoroalkylation on the Desired Position of Organic Molecules
Kitazume, Tomoya,Ishikawa, Nobuo
, p. 5186 - 5191 (2007/10/02)
Perfluoroalkylzinc iodides or bromides wich were prepared from perfluoroalkyl iodides or bromides and zinc powder in N,N-dimethylformamide or tetrahydrofuran with ultrasonic irradiation were found to behave as potential perfluoroalkylating reagents for the preparation of a wide variety of perfluoroalkylated compounds.Especially, the ultrasound-promoted asymmetric induction with perfluoroalkyl group on the asymmetrical carbon was achieved by the reaction of perfluoroalkyl halides with optically active enamines in the presence of zinc powder and a catalytic amount of dichlorobis(?-cyclopentadienyl)titanium.
ULTRASOUND-PROMOTED HYDRPERFLUOROALKYLATION OF ALKYNES WITH PERFLUOROALKYLZINC IODIDE AND COPPER(I) IODIDE
Kitazume, Tomoya,Ishikawa, Nobuo
, p. 1453 - 1454 (2007/10/02)
The reaction of perfluoroalkyl iodides with terminal alkynes and ultrasonically dispersed zinc in the presence of copper(I) iodide proceeded smoothly to give the corresponding vinyl perfluoroalkylides in good yields.
